Variant report

Variant	rs1726887
Chromosome Location	chr12:44696803-44696804
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10506245	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10506246	0.90[YRI][hapmap]
rs1098497	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1527315	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1618337	1.00[AMR][1000 genomes]
rs1622682	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.83[LWK][hapmap];1.00[MKK][hapmap];0.81[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1625442	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs1643432	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs1643433	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1643434	1.00[ASN][1000 genomes]
rs1644007	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs1644009	0.83[ASN][1000 genomes]
rs1644010	0.83[ASN][1000 genomes]
rs1644011	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1644014	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs1716605	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1716606	1.00[ASN][1000 genomes]
rs1716609	1.00[CHB][hapmap]
rs1726874	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs1726879	1.00[ASN][1000 genomes]
rs1726884	1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1726886	1.00[YRI][hapmap]
rs1726888	1.00[ASN][1000 genomes]
rs1726889	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1726890	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1726900	1.00[ASN][1000 genomes]
rs1798020	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[ASN][1000 genomes]
rs1798021	0.82[YRI][hapmap]
rs1798023	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1798025	0.83[ASN][1000 genomes]
rs1798026	0.83[ASN][1000 genomes]
rs1798027	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[ASN][1000 genomes]
rs1798032	1.00[CHB][hapmap]
rs57957351	1.00[AMR][1000 genomes]
rs58523791	1.00[AMR][1000 genomes]
rs58802461	1.00[ASN][1000 genomes]
rs60441308	1.00[ASN][1000 genomes]
rs7314412	1.00[CHB][hapmap]
rs73274196	1.00[AMR][1000 genomes]
rs73274199	1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs73276216	1.00[AMR][1000 genomes]
rs73276236	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73276237	1.00[AMR][1000 genomes]
rs73276240	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73276257	1.00[AMR][1000 genomes]
rs73276275	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73276299	1.00[AMR][1000 genomes]
rs73276302	1.00[AMR][1000 genomes]
rs73278304	1.00[AMR][1000 genomes]
rs73278305	1.00[AMR][1000 genomes]
rs73278320	1.00[AMR][1000 genomes]
rs73278324	1.00[AMR][1000 genomes]
rs73278334	1.00[AMR][1000 genomes]
rs73278339	1.00[AMR][1000 genomes]
rs73278386	1.00[AMR][1000 genomes]
rs7958975	1.00[ASN][1000 genomes]
rs7974460	1.00[CHD][hapmap]
rs840764	1.00[ASN][1000 genomes]
rs840766	1.00[ASN][1000 genomes]
rs840767	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs840768	1.00[ASN][1000 genomes]
rs840772	1.00[CHD][hapmap];0.83[ASN][1000 genomes]
rs840773	1.00[CHB][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs840774	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs859016	1.00[CHB][hapmap];0.82[YRI][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs863482	1.00[CHB][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9738577	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv686	chr12:44671240-44696910	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription	lncRNA	n/a	inside rSNPs	n/a
3	nsv1038498	chr12:44679455-44816572	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44676600-44697800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:44682000-44698600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:44688800-44702000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:44690400-44697800	Weak transcription	HSMMtube	muscle
5	chr12:44690400-44698000	Weak transcription	Liver	Liver
6	chr12:44690400-44698600	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr12:44690600-44697800	Weak transcription	Aorta	Aorta
8	chr12:44690600-44697800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr12:44690800-44698000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr12:44690800-44698000	Weak transcription	Esophagus	oesophagus
11	chr12:44690800-44701400	Weak transcription	Left Ventricle	heart
12	chr12:44691400-44701400	Weak transcription	Psoas Muscle	Psoas
13	chr12:44693600-44697800	Weak transcription	Fetal Intestine Small	intestine
14	chr12:44693600-44698600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:44694200-44697400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr12:44694600-44698200	Weak transcription	Ovary	ovary
17	chr12:44694600-44706000	Weak transcription	Fetal Muscle Trunk	muscle
18	chr12:44694800-44697800	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr12:44695200-44699200	Weak transcription	Brain Anterior Caudate	brain
20	chr12:44696200-44697800	Weak transcription	Pancreas	Pancrea
21	chr12:44696600-44697800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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